Angiopep-2 modified PE-PEG based polymeric micelles for amphotericin B delivery targeted to the brain

被引:171
作者
Shao, Kun [1 ]
Huang, Rongqin [1 ]
Li, Jianfeng [1 ]
Han, Liang [1 ]
Ye, Liya [2 ]
Lou, Jinning [2 ]
Jiang, Chen [1 ]
机构
[1] Fudan Univ, Sch Pharm, Dept Pharmaceut, Shanghai 201203, Peoples R China
[2] China Japan Friendship Hosp, Minist Hlth, Inst Clin Med Sci, Beijing 100029, Peoples R China
关键词
Brain targeting; LRP; Angiopep-2; Polymeric micelles; P-glycoprotein; CENTRAL-NERVOUS-SYSTEM; IMPROVED DRUG SOLUBILIZATION; BLOCK-COPOLYMER MICELLES; POORLY SOLUBLE DRUGS; ENDOTHELIAL-CELLS; MIXED MICELLES; PHOSPHOLIPID MICELLES; FUNCTIONAL-ACTIVITY; VECTOR ANGIOPEP-2; FUNGAL-INFECTIONS;
D O I
10.1016/j.jconrel.2010.06.018
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amphotericin B (AmB) is a poorly water soluble antibiotic and is used to treat fungal infections of the central nervous system (CNS). However, AmB shows poor penetration into the CNS. Angiopep-2, the ligand of low-density lipoprotein receptor-related protein (LRP) present on the BBB, exhibits higher transcytosis capacity and parenchymal accumulation, which allowed us to consider the selectivity of it for receptor-mediated drug targeting to the brain. With this in mind, we prepared angiopep-2 modified PE-PEG based micellar drug delivery system loaded with the antifungal drug AmB to evaluate the efficiency of AmB accumulating into the brain. PE-PEG based micelles as nano-scaled drug carriers were investigated by incorporating AmB with high drug entrapping efficiency, improving solubilization of AmB and reducing its toxicity to mammalian cells. The AmB-incorporated angiopep-2 modified micelles showed highest efficiency in penetrating across the blood-brain barrier (BBB) than unmodified micelles and Fungizone (deoxycholate amphotericin B) in vitro and in vivo. Meanwhile, contrary to the free Rho 123, the enhancement of Rho 123-incorporated angiopep-2 modified micelles across the BBB can be explained by angiopep-2 modified polymeric micelles that have a potential to overcome the activity of efflux proteins expressed on the BBB such as P-glycoprotein. In conclusion, angiopep-2 modified polymeric micelles could be developed as a novel drug delivery system for brain targeting. (C) 2010 Elsevier BM. All rights reserved.
引用
收藏
页码:118 / 126
页数:9
相关论文
共 58 条
[21]   Significant transport of doxorubicin into the brain with polysorbate 80-coated nanoparticles [J].
Gulyaev, AE ;
Gelperina, SE ;
Skidan, IN ;
Antropov, AS ;
Kivman, GY ;
Kreuter, J .
PHARMACEUTICAL RESEARCH, 1999, 16 (10) :1564-1569
[22]   Application of multiple response optimization technique to extended release formulations design [J].
Hamed, E ;
Sakr, A .
JOURNAL OF CONTROLLED RELEASE, 2001, 73 (2-3) :329-338
[23]  
HEGMANN EJ, 1992, CANCER RES, V52, P6969
[24]   Functional characterization of the brain-to-blood efflux clearance of human amyloid-β peptide (1-40) across the rat blood-brain barrier [J].
Ito, Shingo ;
Ohtsuki, Sumio ;
Terasaki, Tetsuya .
NEUROSCIENCE RESEARCH, 2006, 56 (03) :246-252
[25]   Amphotericin B-entrapping lipid nanoparticles and their in vitro and in vivo characteristics [J].
Jung, Suk Hyun ;
Lim, Deok Hwi ;
Jung, Soon Hwa ;
Lee, Jung Eun ;
Jeong, Kyu-Sung ;
Seong, Hasoo ;
Shin, Byung Cheol .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 37 (3-4) :313-320
[26]  
KABANOV AV, 1992, BIOCHEM INT, V26, P1035
[27]   Gene delivery targeted to the brain using an Angiopep-conjugated polyethyleneglycol-modified polyamidoamine dendrimer [J].
Ke, Weilun ;
Shao, Kun ;
Huang, Rongqin ;
Han, Liang ;
Liu, Yang ;
Li, Jianfeng ;
Kuang, Yuyang ;
Ye, Liya ;
Lou, Jinning ;
Jiang, Chen .
BIOMATERIALS, 2009, 30 (36) :6976-6985
[28]   In situ blood-brain barrier transport of nanoparticles [J].
Koziara, JM ;
Lockman, PR ;
Allen, DD ;
Mumper, RJ .
PHARMACEUTICAL RESEARCH, 2003, 20 (11) :1772-1778
[29]   Nanoparticulate systems for brain delivery of drugs [J].
Kreuter, J .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 47 (01) :65-81
[30]   Sterically stabilized phospholipid mixed micelles:: In vitro evaluation as a novel carrier for water-insoluble drugs [J].
Krishnadas, A ;
Rubinstein, I ;
Önyüksel, H .
PHARMACEUTICAL RESEARCH, 2003, 20 (02) :297-302